JP2014198798A - Pressure sensitive adhesive and image display device using the same - Google Patents
Pressure sensitive adhesive and image display device using the same Download PDFInfo
- Publication number
- JP2014198798A JP2014198798A JP2013075184A JP2013075184A JP2014198798A JP 2014198798 A JP2014198798 A JP 2014198798A JP 2013075184 A JP2013075184 A JP 2013075184A JP 2013075184 A JP2013075184 A JP 2013075184A JP 2014198798 A JP2014198798 A JP 2014198798A
- Authority
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- Prior art keywords
- sensitive adhesive
- image display
- pressure
- weight
- meth
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- JSCDRVVVGGYHSN-UHFFFAOYSA-N 8-hydroxyoctyl prop-2-enoate Chemical compound OCCCCCCCCOC(=O)C=C JSCDRVVVGGYHSN-UHFFFAOYSA-N 0.000 description 1
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Images
Classifications
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- G—PHYSICS
- G06—COMPUTING; CALCULATING OR COUNTING
- G06F—ELECTRIC DIGITAL DATA PROCESSING
- G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
- G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
- G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
- G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
- G06F3/0414—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means using force sensing means to determine a position
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J165/00—Adhesives based on macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Adhesives based on derivatives of such polymers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/385—Acrylic polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1808—C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F226/06—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
- C08F226/08—N-Vinyl-pyrrolidine
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- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
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Abstract
Description
本発明は、画像表示パネルの前面に透明板またはタッチパネルを備える画像表示装置の形成に用いられる粘着剤に関する。さらに、本発明は当該粘着剤を用いた画像表示装置の製造方法に関する。 The present invention relates to an adhesive used for forming an image display device including a transparent plate or a touch panel on the front surface of an image display panel. Furthermore, this invention relates to the manufacturing method of the image display apparatus using the said adhesive.
携帯電話、カーナビゲーション装置、パソコン用モニタ、テレビ等の各種画像表示装置として、液晶表示装置や有機ＥＬ表示装置が広く用いられている。画像表示パネル（液晶パネルや有機ＥＬパネル）の外表面からの衝撃による画像表示パネルの破損防止等を目的として、画像表示パネルの視認側に、透明樹脂板やガラス板等の前面透明板（「ウインドウ層」等とも称される）が設けられることがある。また、タッチパネルを備える表示装置では、一般に、画像表示パネルの視認側にタッチパネルが配置されている（以下、前面透明板とタッチパネルとを併せて「前面透明部材」と称する場合がある）。 Liquid crystal display devices and organic EL display devices are widely used as various image display devices such as mobile phones, car navigation devices, personal computer monitors, and televisions. For the purpose of preventing damage to the image display panel due to impact from the outer surface of the image display panel (liquid crystal panel or organic EL panel), a transparent front plate such as a transparent resin plate or glass plate (“ Also referred to as “window layer” or the like. In a display device including a touch panel, the touch panel is generally disposed on the viewing side of the image display panel (hereinafter, the front transparent plate and the touch panel may be collectively referred to as “front transparent member”).
このように、画像表示パネルの視認側に前面透明板やタッチパネル等の前面透明部材が配置される場合、パネル表面を保護するため、これらの層間に０．５〜１．５ｍｍ程度の空隙を設けるエアーギャップ構造（中空構造）を構成することが行われている。しかし、エアーギャップ構造部分の空気の屈折率が約１であるのに対して、画像表示パネルの偏光板や前面透明部材等を構成するプラスチック材料やガラス材料の屈折率は１．５程度であるため、界面での反射や屈折が大きくなる。そのため、エアーギャップ構造を有する画像表示装置では、画像表示パネルから発した映像光の拡散・散乱や、太陽光等の外光反射が生じやすく、画像表示装置の視認性を低下させるとの問題がある。 Thus, when a front transparent member such as a front transparent plate or a touch panel is disposed on the viewing side of the image display panel, a gap of about 0.5 to 1.5 mm is provided between these layers in order to protect the panel surface. An air gap structure (hollow structure) is configured. However, while the refractive index of air in the air gap structure portion is about 1, the refractive index of the plastic material or glass material constituting the polarizing plate or front transparent member of the image display panel is about 1.5. Therefore, reflection and refraction at the interface increase. Therefore, in the image display device having an air gap structure, there is a problem that the visibility and the visibility of the image display device are lowered because diffusion and scattering of image light emitted from the image display panel and reflection of external light such as sunlight are likely to occur. is there.
上記のような問題を解消するため、近年、上記エアーギャップ構造部分に、ガラスや樹脂等と屈折率が近い透明な光学樹脂を充填する「層間充填構造」が提案されている（例えば、特許文献１，２参照）。層間充填構造では、上記エアーギャップ内に光学樹脂が充填されることにより、界面の屈折率差が減少するため、反射や散乱に起因する視認性の低下が抑制される。また、エアーギャップ内に光学樹脂が充填されることにより、画像表示装置全体の強度が増すため、万が一、前面透明板等が破損した場合であっても、その形成材料であるガラス等が飛散することを防ぐといった効果も得られる。さらに、層間充填剤を構成する光学樹脂として粘着剤を用いることで、画像表示パネルと前面透明部材とを接着して固着することができる。 In order to solve the above problems, in recent years, an “interlayer filling structure” has been proposed in which the air gap structure portion is filled with a transparent optical resin having a refractive index close to that of glass, resin, or the like (for example, Patent Documents). 1 and 2). In the interlayer filling structure, the optical resin is filled in the air gap, so that the difference in the refractive index at the interface is reduced, so that a decrease in visibility due to reflection and scattering is suppressed. Moreover, since the strength of the entire image display device is increased by filling the air gap with the optical resin, even if the front transparent plate or the like is broken, the forming material glass or the like is scattered. The effect of preventing this is also obtained. Further, by using an adhesive as the optical resin constituting the interlayer filler, the image display panel and the front transparent member can be bonded and fixed.
前面透明部材の画像表示パネル側の面の周縁部には、装飾や光遮蔽を目的とした印刷が施されることが多い。周縁部に印刷が施されると、印刷部分の境界に、１０μｍ〜数十μｍ程度の段差が生じるが、層間充填剤としてシート状粘着剤を用いた際は、この印刷段差部に気泡が生じ易いとの問題が生じ得る。かかる問題に鑑み、特許文献３では、粘着材の弾性率を所定範囲として、貼り合わせ時の粘着材に流動性を持たせることによって、段差追従性（段差吸収性）を付与し、印刷段差部周辺の気泡発生を抑制することが提案されている。 Printing for the purpose of decoration or light shielding is often performed on the peripheral edge of the surface of the front transparent member on the image display panel side. When printing is performed on the peripheral portion, a step of about 10 μm to several tens of μm occurs at the boundary of the printed portion. When a sheet-like adhesive is used as an interlayer filler, bubbles are generated in the printed step portion. The problem of being easy can arise. In view of such a problem, in Patent Document 3, the adhesive material at the time of bonding is given fluidity by setting the elastic modulus of the adhesive material to a predetermined range, thereby providing step followability (step absorbability) and printing step portion. It has been proposed to suppress peripheral bubble generation.
上記特許文献３で提案されているように、粘着剤の流動性を高めることが、印刷段差部周辺の気泡の抑制に有効である。粘着材の流動性を高める方法としては、粘着材を構成するベースポリマーの低分子量化や架橋度低下等が一般的である。しかしながら、ベースポリマーの低分子量化や架橋度低下を行うと、粘着剤層の移着や、端面からのはみ出しが生じ易くなり、作業性の低下や周囲の汚染を招く傾向がある。すなわち、一般に、段差追従性を高めようとすると、粘着剤のハンドリング性が低下する傾向がある。 As proposed in Patent Document 3, increasing the fluidity of the pressure-sensitive adhesive is effective for suppressing bubbles around the printing step portion. As a method for increasing the fluidity of the pressure-sensitive adhesive material, it is common to lower the molecular weight of the base polymer constituting the pressure-sensitive adhesive material or to reduce the degree of crosslinking. However, when the molecular weight of the base polymer is lowered or the degree of crosslinking is reduced, transfer of the pressure-sensitive adhesive layer and protrusion from the end surface are liable to occur, and there is a tendency for workability and surrounding contamination to be caused. That is, in general, when trying to improve the step following property, the handling property of the adhesive tends to be lowered.
また、層間充填剤を設けた画像表示パネルが、高温高湿環境に長時間曝されると、層間充填剤が白濁するとの問題を生じ得る。上記特許文献３では、層間充填剤（粘着剤）を構成するベースポリマーが、極性基含有モノマー成分を含有する場合に、白濁を解消し得ることが記載されている。しかしながら、極性の高いベースポリマーは流動性が低いため、段差追従性が低く、上述の気泡の問題を生じ易くなる。そのため、層間充填剤として用いられた場合における、段差追従性とハンドリング性とを両立し、かつ高温高湿環境下での白濁を生じ難い光学粘着剤の開発が望まれている。 Further, when the image display panel provided with the interlayer filler is exposed to a high temperature and high humidity environment for a long time, a problem may occur that the interlayer filler becomes cloudy. In the said patent document 3, when the base polymer which comprises an interlayer filler (adhesive) contains a polar group containing monomer component, it describes that white turbidity can be eliminated. However, since the highly polar base polymer has low fluidity, the step following ability is low, and the above-described bubble problem is likely to occur. Therefore, there is a demand for the development of an optical pressure-sensitive adhesive that achieves both step followability and handling properties when used as an interlayer filler and hardly causes white turbidity in a high temperature and high humidity environment.
上記課題に鑑みて検討の結果、所定のポリマーと粘着付与剤とを含有する粘着剤が、通常の取扱い時のハンドリング性が良好であり、かつ段差追従性に優れ、さらに白濁の発生が抑制されることを見出し、本発明に至った。 As a result of examination in view of the above problems, the pressure-sensitive adhesive containing a predetermined polymer and a tackifier has good handling properties during normal handling, excellent step following performance, and further suppresses the occurrence of white turbidity. As a result, the present invention has been achieved.
本発明は、前面透明板とタッチパネルとの間、前面透明板と画像表示パネルとの間、またはタッチパネルと画像表示パネルとの間に配置して用いられる粘着剤に関する。本発明の粘着剤は、アクリル系ベースポリマーと、軟化点が７０℃〜１５０℃の水素添加型テルペンフェノール樹脂とを含有する。水素添加型テルペンフェノール樹脂は、テルペンのモル比率が０．１〜０．７であることが好ましい。 The present invention relates to an adhesive used by being disposed between a front transparent plate and a touch panel, between a front transparent plate and an image display panel, or between a touch panel and an image display panel. The pressure-sensitive adhesive of the present invention contains an acrylic base polymer and a hydrogenated terpene phenol resin having a softening point of 70 ° C to 150 ° C. The hydrogenated terpene phenol resin preferably has a terpene molar ratio of 0.1 to 0.7.
粘着剤組成物の全量１００重量部に対する、アクリル系ベースポリマーの含有量は、４５〜９５重量部が好ましい。また、アクリル系ベースポリマーと水素添加型テルペンフェノール樹脂の含有量の合計は、７０重量部以上が好ましい。アクリル系ベースポリマーは、構成モノマー成分全量に対する極性モノマーユニットの含有率が、３〜５０重量％であることが好ましい。 As for content of an acrylic base polymer with respect to 100 weight part of whole quantity of an adhesive composition, 45-95 weight part is preferable. The total content of the acrylic base polymer and the hydrogenated terpene phenol resin is preferably 70 parts by weight or more. In the acrylic base polymer, the content of the polar monomer unit with respect to the total amount of the constituent monomer components is preferably 3 to 50% by weight.
さらに、本発明は、画像表示装置に関する。本発明の画像表示装置は、画像表示パネルの表面に、タッチパネルおよび前面透明板の少なくとも一方を備え、前面透明板とタッチパネルとの間、前面透明板と画像表示パネルとの間、およびタッチパネルと画像表示パネルとの間のいずれかに、前記粘着剤からなる粘着剤層を備える。 Furthermore, the present invention relates to an image display device. The image display device of the present invention includes at least one of a touch panel and a front transparent plate on the surface of the image display panel, between the front transparent plate and the touch panel, between the front transparent plate and the image display panel, and between the touch panel and the image. A pressure-sensitive adhesive layer made of the pressure-sensitive adhesive is provided between the display panel and the display panel.
本発明の粘着剤は、所定の粘着付与剤を含有するため、層間充填剤として用いられた場合に、ハンドリング性に優れ、段差追従性を有するとともに、高温高湿環境下での白濁が生じ難い。そのため、本発明の粘着剤は、前面透明板とタッチパネルとの間、前面透明板と画像表示パネルとの間、またはタッチパネルと画像表示パネルとの間の層間充填剤として、画像表示装置の形成に好適に用いられる。 Since the pressure-sensitive adhesive of the present invention contains a predetermined tackifier, when used as an interlayer filler, it has excellent handling properties, has step-following properties, and is less prone to white turbidity in a high-temperature, high-humidity environment. . Therefore, the adhesive of the present invention is used for forming an image display device as an interlayer filler between the front transparent plate and the touch panel, between the front transparent plate and the image display panel, or between the touch panel and the image display panel. Preferably used.
本発明の粘着剤は、画像表示パネルとタッチパネルとの間、タッチパネルと前面透明板との間、画像表示パネルと前面透明板との間等の層間充填剤として用いられる。 The pressure-sensitive adhesive of the present invention is used as an interlayer filler between the image display panel and the touch panel, between the touch panel and the front transparent plate, and between the image display panel and the front transparent plate.
図１は、本発明の粘着剤の一使用形態にかかる画像表示装置を模式的に表す断面図である。図１に示す画像表示装置１００では、液晶パネルや有機ＥＬパネル等の画像表示パネル１０の表面に、タッチパネル３０および前面透明板７０を備える。画像表示パネル１０とタッチパネル３０との間の粘着剤層２１やタッチパネル３０と前面透明板７０の粘着剤層２２は、いわゆる「層間充填剤」であり、各部材の固着に加えて、界面の屈折率差を低減し、光の反射や散乱に起因する視認性の低下を抑制する機能を有する。また、層間充填剤は、タッチパネル３０や画像表示パネル１０への外表面からの衝撃や押圧に対するクッション層としての作用も有する。
FIG. 1 is a cross-sectional view schematically showing an image display device according to one usage pattern of the pressure-sensitive adhesive of the present invention. The
［粘着剤の組成］
本発明の粘着剤は、ベースポリマーおよび粘着付与剤を含有する。
[Adhesive composition]
The pressure-sensitive adhesive of the present invention contains a base polymer and a tackifier.
ベースポリマーとしては、アクリル系ポリマーを主成分とするものが用いられる。アクリル系ポリマーは、光学透明性および接着性に優れ、かつ適度な柔軟性を有する。アクリル系ベースポリマーとしては、（メタ）アクリル酸アルキルエステルのモノマーユニットを主骨格とするものが用いられる。なお、本明細書において、「（メタ）アクリル」とは、アクリルおよび／またはメタクリルを意味する。 As a base polymer, what has an acrylic polymer as a main component is used. The acrylic polymer is excellent in optical transparency and adhesiveness, and has appropriate flexibility. As the acrylic base polymer, one having a monomer unit of (meth) acrylic acid alkyl ester as a main skeleton is used. In the present specification, “(meth) acryl” means acryl and / or methacryl.
前記（メタ）アクリル酸アルキルエステルとしては、アルキル基の炭素数が１〜２０である（メタ）アクリル酸アルキルエステルが好適に用いられる。例えば、（メタ）アクリル酸メチル、（メタ）アクリル酸エチル、（メタ）アクリル酸ブチル、（メタ）アクリル酸イソブチル、（メタ）アクリル酸ｓ−ブチル、（メタ）アクリル酸ｔ−ブチル、（メタ）アクリル酸ペンチル、（メタ）アクリル酸イソペンチル、（メタ）アクリル酸ネオペンチル、（メタ）アクリル酸ヘキシル、（メタ）アクリル酸ヘプチル、（メタ）アクリル酸２−エチルヘキシル、（メタ）アクリル酸オクチル、（メタ）アクリル酸イソオクチル、（メタ）アクリル酸ノニル、（メタ）アクリル酸イソノニル、（メタ）アクリル酸デシル、（メタ）アクリル酸イソデシル、（メタ）アクリル酸ウンデシル、（メタ）アクリル酸ドデシル、（メタ）アクリル酸イソトリドデシル、（メタ）アクリル酸テトラデシル、（メタ）アクリル酸イソテトラデシル、（メタ）アクリル酸ペンタデシル、（メタ）アクリル酸セチル、（メタ）アクリル酸ヘプタデシル、（メタ）アクリル酸オクタデシル、（メタ）アクリル酸イソオクタデシル、（メタ）アクリル酸ノナデシル、（メタ）アクリル酸アラキル等が挙げられる。 As said (meth) acrylic-acid alkylester, the (meth) acrylic-acid alkylester whose carbon number of an alkyl group is 1-20 is used suitably. For example, methyl (meth) acrylate, ethyl (meth) acrylate, butyl (meth) acrylate, isobutyl (meth) acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, (meta ) Pentyl acrylate, isopentyl (meth) acrylate, neopentyl (meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, ( Isooctyl acrylate, nonyl (meth) acrylate, isononyl (meth) acrylate, decyl (meth) acrylate, isodecyl (meth) acrylate, undecyl (meth) acrylate, dodecyl (meth) acrylate, (meth) ) Isotridodecyl acrylate, tetradecyl (meth) acrylate, (meta Isotetradecyl acrylate, pentadecyl (meth) acrylate, cetyl (meth) acrylate, heptadecyl (meth) acrylate, octadecyl (meth) acrylate, isooctadecyl (meth) acrylate, nonadecyl (meth) acrylate, ( Examples include araalkyl methacrylate.
粘着剤の流動性を高める等の目的で、アクリル系ベースポリマーは、前記（メタ）アクリル酸アルキルエステルのモノマーユニットとして、アルキル基が分枝を有する（メタ）アクリル酸アルキルエステルを含有することが好ましい。前記例示のモノマーの中でも、分枝アルキル（メタ）アクリル酸エステルとしては、（メタ）アクリル酸２−エチルヘキシル、（メタ）アクリル酸イソオクチル、（メタ）アクリル酸イソノニル、（メタ）アクリル酸イソデシル、（メタ）アクリル酸イソテトラデシル、（メタ）アクリル酸イソオクタデシル等が好適に用いられる。なお、分枝アルキル（メタ）アクリル酸エステルは２種以上を併用することもできる。また、これらの分枝アルキル（メタ）アクリル酸エステルは、直鎖アルキル（メタ）アクリル酸エステルと併用して用いられてもよい。 For the purpose of increasing the fluidity of the pressure-sensitive adhesive, the acrylic base polymer may contain a (meth) acrylic acid alkyl ester having a branched alkyl group as a monomer unit of the (meth) acrylic acid alkyl ester. preferable. Among the exemplified monomers, examples of the branched alkyl (meth) acrylate include 2-ethylhexyl (meth) acrylate, isooctyl (meth) acrylate, isononyl (meth) acrylate, isodecyl (meth) acrylate, ( (Meth) isotetradecyl acrylate, isooctadecyl (meth) acrylate and the like are preferably used. In addition, 2 or more types of branched alkyl (meth) acrylic acid esters can be used in combination. Moreover, these branched alkyl (meth) acrylic acid esters may be used in combination with a linear alkyl (meth) acrylic acid ester.
上記（メタ）アクリル酸アルキルエステルの含有量は、ベースポリマーを構成するモノマー成分全量に対して４０重量％以上であることが好ましく、より好ましくは５０重量％以上、さらに好ましくは６０重量％以上である。（メタ）アクリル酸アルキルエステル成分全量に対する、アルキル基が分枝を有する（メタ）アクリル酸アルキルエステルの含有量は、５０重量％以上が好ましく、６０重量％以上がより好ましい。 The content of the (meth) acrylic acid alkyl ester is preferably 40% by weight or more, more preferably 50% by weight or more, and still more preferably 60% by weight or more based on the total amount of monomer components constituting the base polymer. is there. The content of the alkyl (meth) acrylate having a branched alkyl group with respect to the total amount of the (meth) acrylic acid alkyl ester component is preferably 50% by weight or more, and more preferably 60% by weight or more.
ベースポリマーを構成するアクリル系ポリマーは、上記の（メタ）アクリル酸アルキルエステルに加えて、極性の高いモノマーユニットを含有することが好ましい。ベースポリマーが高極性モノマーユニットを含有することにより、層間充填剤として用いられた場合の、高温高湿下での粘着剤の白濁が抑制される。高極性モノマーユニットとしては、ヒドロキシ基含有モノマーや窒素含有モノマーが好ましい。 The acrylic polymer constituting the base polymer preferably contains a highly polar monomer unit in addition to the above (meth) acrylic acid alkyl ester. When the base polymer contains a high-polarity monomer unit, white turbidity of the pressure-sensitive adhesive under high temperature and high humidity when used as an interlayer filler is suppressed. As the highly polar monomer unit, a hydroxy group-containing monomer or a nitrogen-containing monomer is preferable.
ヒドロキシ基含有モノマーとしては、（メタ）アクリル酸２−ヒドロキシエチル、（メタ）アクリル酸２−ヒドロキシプロピル、（メタ）アクリル酸４−ヒドロキシブチル、（メタ）アクリル酸６−ヒドロキシヘキシル、（メタ）アクリル酸８−ヒドロキシオクチル、（メタ）アクリル酸１０−ヒドロキシデシル、（メタ）アクリル酸１２−ヒドロキシラウリルや（４−ヒドロキシメチルシクロヘキシル）−メチルアクリレート等のアルコール性ヒドロキシ基含有（メタ）アクリル酸エステルが好ましく用いられる。 Examples of the hydroxy group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, (meth) Alcoholic hydroxy group-containing (meth) acrylic esters such as 8-hydroxyoctyl acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate and (4-hydroxymethylcyclohexyl) -methyl acrylate Is preferably used.
窒素含有モノマーとしては、Ｎ−ビニルピロリドン、メチルビニルピロリドン、ビニルピリジン、ビニルピペリドン、ビニルピリミジン、ビニルピペラジン、ビニルピラジン、ビニルピロール、ビニルイミダゾール、ビニルオキサゾール、ビニルモルホリン、Ｎ−ビニルカルボン酸アミド類、Ｎ−ビニルカプロラクタム等が挙げられる。 Examples of nitrogen-containing monomers include N-vinyl pyrrolidone, methyl vinyl pyrrolidone, vinyl pyridine, vinyl piperidone, vinyl pyrimidine, vinyl piperazine, vinyl pyrazine, vinyl pyrrole, vinyl imidazole, vinyl oxazole, vinyl morpholine, N-vinyl carboxylic acid amides, N -Vinyl caprolactam etc. are mentioned.
ベースポリマー中の高極性モノマー成分の割合は特に制限されないが、構成モノマー成分全量に対して、３〜５０重量％が好ましく、５〜３０重量％がより好ましい。高極性モノマーの含有量が３重量％以上であれば、高温高湿環境での粘着剤の白濁が抑制される傾向がある。また、極性モノマーの含有量が５０重量％以下であれば、粘着剤が適度の柔軟性を有し、段差追従性を有し得る。 Although the ratio of the highly polar monomer component in the base polymer is not particularly limited, it is preferably 3 to 50% by weight and more preferably 5 to 30% by weight with respect to the total amount of the constituent monomer components. If the content of the highly polar monomer is 3% by weight or more, the white turbidity of the pressure-sensitive adhesive in a high temperature and high humidity environment tends to be suppressed. Moreover, if content of a polar monomer is 50 weight% or less, an adhesive has moderate softness | flexibility and can have level | step difference followable | trackability.
ベースポリマーが、（メタ）アクリル酸アルキルエステルと上記高極性モノマーとの共重合体である場合、構成モノマーの並びはランダムであっても、ブロックであってもかまわない。また、ベースポリマーは、複数種の（メタ）アクリル酸アルキルエステルや、複数種の高極性モノマーの共重合体であってもよい。 When the base polymer is a copolymer of (meth) acrylic acid alkyl ester and the above-mentioned highly polar monomer, the arrangement of the constituent monomers may be random or block. The base polymer may be a copolymer of a plurality of types of (meth) acrylic acid alkyl esters or a plurality of types of highly polar monomers.
上記のアクリル系ポリマーは、上記モノマー成分を公知慣用の重合方法により重合して調製することができる。アクリル系ポリマーの重合方法としては、例えば、溶液重合法、乳化重合法、塊状重合法や活性エネルギー線照射による重合（活性エネルギー線重合法）等が挙げられる。透明性、耐水性、コスト等の点で、溶液重合法、または活性エネルギー線重合法が好ましい。 The acrylic polymer can be prepared by polymerizing the monomer component by a known and usual polymerization method. Examples of the polymerization method of the acrylic polymer include solution polymerization method, emulsion polymerization method, bulk polymerization method, polymerization by active energy ray irradiation (active energy ray polymerization method) and the like. From the viewpoint of transparency, water resistance, cost, etc., the solution polymerization method or the active energy ray polymerization method is preferable.
上記のアクリル系ポリマーの調製に際しては、重合反応の種類に応じて、光重合開始剤（光開始剤）や熱重合開始剤等の重合開始剤を用いてもよい。重合開始剤は単独で、又は２種以上を組み合わせて使用することができる。光重合開始剤の使用量は、特に制限はされないが、例えば、アクリル系ベースポリマーを形成するモノマー成分全量１００重量部に対して０．０１〜０．５重量部が好ましく、より好ましくは０．０５〜０．３重量部である。 In preparing the acrylic polymer, a polymerization initiator such as a photopolymerization initiator (photoinitiator) or a thermal polymerization initiator may be used depending on the type of polymerization reaction. A polymerization initiator can be used individually or in combination of 2 or more types. Although the usage-amount of a photoinitiator is not restrict | limited in particular, For example, 0.01-0.5 weight part is preferable with respect to 100 weight part of monomer components whole quantity which forms an acryl-type base polymer, More preferably, it is 0.8. It is 05-0.3 weight part.
ベースポリマーの分子量は、適宜に調整されるが、例えば、ポリスチレン換算の重量平均分子量が５万〜２００万程度、好ましくは、７万〜１８０万程度である。 Although the molecular weight of a base polymer is adjusted suitably, For example, the weight average molecular weight of polystyrene conversion is about 50,000-2 million, Preferably, it is about 70,000-1,800,000.
本発明の粘着剤は、上記ベースポリマーが、必要に応じて架橋構造を有していてもよい。架橋構造の形成は、例えば、ベースポリマーの重合後に、架橋剤を添加することにより行われる。架橋剤としては、イソシアネート系架橋剤、エポキシ系架橋剤、オキサゾリン系架橋剤、アジリジン系架橋剤、カルボジイミド系架橋剤、金属キレート系架橋剤等の一般に用いられているものを使用できる。 In the pressure-sensitive adhesive of the present invention, the base polymer may have a crosslinked structure as necessary. Formation of a crosslinked structure is performed, for example, by adding a crosslinking agent after polymerization of the base polymer. As the crosslinking agent, generally used ones such as an isocyanate crosslinking agent, an epoxy crosslinking agent, an oxazoline crosslinking agent, an aziridine crosslinking agent, a carbodiimide crosslinking agent, and a metal chelate crosslinking agent can be used.
架橋剤の含有量は、アクリル系ベースポリマー１００重量部に対して、通常、０〜１０重量部の範囲であり、好ましくは０〜５重量部である。架橋剤の含有量が多すぎると、粘着剤の柔軟性が低下し、被着体への密着性が低下する場合がある。粘着剤組成物として架橋剤が用いられる場合、架橋構造を形成するために加熱工程を経るのが好ましい。加熱温度や加熱時間は、使用する架橋剤の種類に応じて適宜設定されるが、通常、２０℃〜１６０℃の範囲で、１分から７日程度の加熱により架橋が行われる。 The content of the crosslinking agent is usually in the range of 0 to 10 parts by weight, preferably 0 to 5 parts by weight with respect to 100 parts by weight of the acrylic base polymer. When there is too much content of a crosslinking agent, the softness | flexibility of an adhesive will fall and the adhesiveness to a to-be-adhered body may fall. When a crosslinking agent is used as the pressure-sensitive adhesive composition, it is preferable to undergo a heating step in order to form a crosslinked structure. The heating temperature and heating time are appropriately set according to the type of the crosslinking agent to be used, but are usually crosslinked by heating in the range of 20 ° C. to 160 ° C. for about 1 minute to 7 days.
粘着剤中には、接着力の調整等を目的として、各種のシランカップリング剤を添加することもできる。粘着剤にシランカップリング剤が添加される場合、その添加量は、アクリル系ベースポリマー１００重量部に対して、通常０．０１〜５．０重量部程度であり、０．０３〜２．０重量部程度が好ましい。 Various silane coupling agents can be added to the pressure-sensitive adhesive for the purpose of adjusting the adhesive strength. When a silane coupling agent is added to the pressure-sensitive adhesive, the addition amount is usually about 0.01 to 5.0 parts by weight with respect to 100 parts by weight of the acrylic base polymer, and 0.03 to 2.0. About parts by weight are preferred.
本発明の粘着剤は、上記のアクリル系ベースポリマー以外に、シリコーン系ポリマー、ポリエステル、ポリウレタン、ポリアミド、ポリビニルエーテル、酢酸ビニル／塩化ビニルコポリマー、変性ポリオレフィン、エポキシ系、フッ素系、天然ゴム、合成ゴム等のゴム系等のポリマーを含有してもよい。層間充填剤として求められる透明性、段差追従性等を付与する観点から、粘着剤組成物の全量１００重量部に対する上記アクリル系ベースポリマーの含有量は４５重量％以上が好ましく、５０重量％以上がより好ましく、５５重量％以上がさらに好ましい。 In addition to the above acrylic base polymer, the pressure-sensitive adhesive of the present invention is a silicone polymer, polyester, polyurethane, polyamide, polyvinyl ether, vinyl acetate / vinyl chloride copolymer, modified polyolefin, epoxy, fluorine, natural rubber, synthetic rubber. A rubber-based polymer or the like may be contained. From the viewpoint of imparting the transparency required for the interlayer filler, the step following ability, etc., the content of the acrylic base polymer with respect to 100 parts by weight of the total amount of the pressure-sensitive adhesive composition is preferably 45% by weight or more, and 50% by weight or more. More preferred is 55% by weight or more.
本発明の粘着剤は、上記アクリル系ベースポリマーに加えて、粘着付与剤を含有する。粘着付与剤としては、水素添加型テルペンフェノール樹脂が用いられる。水素添加型テルペンフェノール樹脂の軟化点は、７０〜１５０℃が好ましく、７０℃〜１４０℃がより好ましい。軟化点は、ＪＩＳ Ｋ２２０７「環球式軟化点試験方法」により測定することができる。 The pressure-sensitive adhesive of the present invention contains a tackifier in addition to the acrylic base polymer. As the tackifier, a hydrogenated terpene phenol resin is used. The softening point of the hydrogenated terpene phenol resin is preferably 70 to 150 ° C, more preferably 70 to 140 ° C. The softening point can be measured by JIS K2207 “Ring and Ball Softening Point Test Method”.
粘着付与剤としての水素添加型テルペンフェノール樹脂の軟化点が上記範囲であれば、粘着剤の弾性率に所期の温度依存性が付与され得る。すなわち、常温では弾性率が高く（流動性が低く）、粘着剤層の移着や端面からのはみ出しを抑止しつつ、層間充填剤としての被着体との貼り合わせの際の加熱環境では、粘着剤の弾性率が低く（流動性が高く）段差追従性が付与され得る。 If the softening point of the hydrogenated terpene phenol resin as the tackifier is within the above range, the desired temperature dependence can be imparted to the elastic modulus of the adhesive. In other words, the elastic modulus is high at room temperature (low fluidity), while suppressing the transfer of the adhesive layer and the protrusion from the end surface, in the heating environment at the time of bonding with the adherend as an interlayer filler, The elastic modulus of the pressure-sensitive adhesive is low (high fluidity), and step following ability can be imparted.
水素添加型テルペンフェノール樹脂は、テルペンのモル比率が０．１〜０．７であることが好ましく、０．２〜０．６であることがより好ましい。テルペンのモル比率が前記範囲の水素添加型テルペンフェノール樹脂は、上記の極性基含有アクリルベースポリマーとの相溶性に優れる。そのため、所定の軟化点を有し、かつテルペン含有率が所定範囲の水素添加型テルペンフェノール樹脂を、粘着付与剤として用いることにより、高温高湿環境における白濁が抑制され、かつ段差追従性を有する粘着剤が得られる。上記水素添加型テルペンフェノール樹脂は、フェノール部のベンゼン環も水素添加されたものが好ましい。ベンゼン環が水素添加されることにより、より無色透明に近付くとともに、耐熱性が向上する傾向がある。水素添加型テルペンフェノール樹脂の市販品としては、ヤスハラケミカル社製の商品名「ＹＳポリスターＮＨ」等を用いることができる。 The hydrogenated terpene phenol resin preferably has a terpene molar ratio of 0.1 to 0.7, and more preferably 0.2 to 0.6. A hydrogenated terpene phenol resin having a terpene molar ratio within the above range is excellent in compatibility with the above-mentioned polar group-containing acrylic base polymer. Therefore, by using a hydrogenated terpene phenol resin having a predetermined softening point and a terpene content in a predetermined range as a tackifier, white turbidity in a high-temperature and high-humidity environment is suppressed, and has step following ability. An adhesive is obtained. The hydrogenated terpene phenol resin is preferably one in which the benzene ring of the phenol part is also hydrogenated. When the benzene ring is hydrogenated, it tends to be more colorless and transparent and the heat resistance tends to be improved. As a commercial product of the hydrogenated terpene phenol resin, trade name “YS Polystar NH” manufactured by Yashara Chemical Co., Ltd. can be used.
前記範囲の軟化点を有し、かつ極性基を含有するアクリル系ベースポリマーとの相溶性を持たせる観点から、水素添加型テルペンフェノール樹脂の重量平均分子量は２００〜５０００程度が好ましく、５００〜３０００程度がより好ましい。 From the viewpoint of having a softening point in the above range and having compatibility with an acrylic base polymer containing a polar group, the weight average molecular weight of the hydrogenated terpene phenol resin is preferably about 200 to 5,000, more preferably 500 to 3,000. The degree is more preferable.
粘着剤組成物の全量１００重量部に対する上記水素添加型テルペンフェノール樹脂の含有量は、５〜５５重量部が好ましく、１０〜５０重量部がより好ましく、１５〜４５重量部がさらに好ましい。また、粘着剤組成物の全量１００重量部に対する上記アクリル系ベースポリマーと水素添加型テルペンフェノール樹脂の含有量の合計は、７０重量部以上が好ましく、８０重量部以上がより好ましく、８５重量部以上がさらに好ましい。アクリル系ベースポリマーと水素添加型テルペンフェノール樹脂の含有量の合計が過度に小さいと、粘着力や透明性の低下等を招く場合がある。 The content of the hydrogenated terpene phenol resin with respect to 100 parts by weight of the total pressure-sensitive adhesive composition is preferably 5 to 55 parts by weight, more preferably 10 to 50 parts by weight, and still more preferably 15 to 45 parts by weight. Further, the total content of the acrylic base polymer and the hydrogenated terpene phenol resin with respect to 100 parts by weight of the total pressure-sensitive adhesive composition is preferably 70 parts by weight or more, more preferably 80 parts by weight or more, and 85 parts by weight or more. Is more preferable. If the total content of the acrylic base polymer and the hydrogenated terpene phenol resin is excessively small, the adhesive strength and transparency may be lowered.
粘着剤層中には、必要に応じて上記の水素添加型テルペンフェノール樹脂以外の粘着付与剤を添加してもよい。例えば、テルペン系粘着付与剤、スチレン系粘着付与剤、フェノール系粘着付与剤、ロジン系粘着付与剤、エポキシ系粘着付与剤、ジシクロペンタジエン系粘着付与剤、ポリアミド系粘着付与剤、ケトン系粘着付与剤、エラストマー系粘着付与剤等を用いることができる。透明性を確保する観点から、これらの粘着付与剤も水素添加型のものが好ましく用いられる。また、スチレン系の粘着付与剤として、ベンゼン環の一部または全部が水添されたものを用いることもできる。 In the pressure-sensitive adhesive layer, a tackifier other than the above hydrogenated terpene phenol resin may be added as necessary. For example, terpene tackifier, styrene tackifier, phenol tackifier, rosin tackifier, epoxy tackifier, dicyclopentadiene tackifier, polyamide tackifier, ketone tackifier An agent, an elastomer-based tackifier, and the like can be used. From the viewpoint of ensuring transparency, a hydrogenated type of these tackifiers is preferably used. In addition, a styrene-based tackifier having a benzene ring partially or wholly hydrogenated can also be used.
粘着剤中に、水素添加型テルペンフェノール樹脂以外の粘着付与剤を含有する場合、その軟化点は、７０〜１５０℃が好ましく、７０℃〜１４０℃がより好ましい。粘着剤の白濁を抑止する観点から、水素添加型テルペンフェノール樹脂以外の粘着付与剤の含有量は、粘着剤組成物の全固形分１００重量部に対して、１０重量部以下が好ましく、５重量部以下がより好ましく、３重量部以下がさらに好ましい。 When the tackifier contains a tackifier other than the hydrogenated terpene phenol resin, the softening point is preferably 70 to 150 ° C, and more preferably 70 to 140 ° C. From the viewpoint of suppressing the white turbidity of the pressure-sensitive adhesive, the content of the tackifier other than the hydrogenated terpene phenol resin is preferably 10 parts by weight or less with respect to 100 parts by weight of the total solid content of the pressure-sensitive adhesive composition. Part or less is more preferable, and 3 parts by weight or less is more preferable.
本発明の粘着剤は、硬化のタイミングの制御や、確実性等の観点から、光硬化性であることが好ましい。光硬化の方法としては、光硬化性モノマーまたは光硬化性オリゴマーと光ラジカル発生剤を含有する系に、紫外線等の活性光線を照射する方法が好ましい。特に、光感度の高さや、選択できる材料が豊富であることから、エチレン性不飽和化合物と光ラジカル発生剤を用いたシステムが好ましい。光硬化性のエチレン性不飽和化合物は、単官能化合物であってもよく、多官能化合物であってもよい。 The pressure-sensitive adhesive of the present invention is preferably photocurable from the viewpoint of control of the timing of curing and certainty. As a photocuring method, a method of irradiating a system containing a photocurable monomer or photocurable oligomer and a photoradical generator with actinic rays such as ultraviolet rays is preferable. In particular, a system using an ethylenically unsaturated compound and a photo radical generator is preferable because of high photosensitivity and abundant materials that can be selected. The photocurable ethylenically unsaturated compound may be a monofunctional compound or a polyfunctional compound.
光硬化性のモノマーまたはオリゴマーは、２種以上が併用されてもよい。光硬化性粘着剤を構成するためには、上記光硬化性化合物を、粘着剤組成物中にモノマー又はオリゴマーとして存在させる必要がある。そのため、ベースポリマーを重合後、系中に光硬化性化合物が添加されることが好ましい。 Two or more photocurable monomers or oligomers may be used in combination. In order to constitute the photocurable pressure-sensitive adhesive, the photocurable compound needs to be present as a monomer or oligomer in the pressure-sensitive adhesive composition. Therefore, it is preferable that a photocurable compound is added to the system after polymerizing the base polymer.
本発明の粘着剤が光硬化性粘着剤である場合、光硬化性化合物の含有量は、粘着剤組成物の全固形分１００重量部に対して、２〜５０重量部が好ましく、５〜３０重量部がより好ましい。光硬化性化合物の含有量が過度に大きいと、硬化前の粘着剤の流動性が高くなり、ハンドリング性の低下や汚染を招く場合がある。 When the adhesive of this invention is a photocurable adhesive, 2-50 weight part is preferable with respect to 100 weight part of total solids of an adhesive composition, and, as for content of a photocurable compound, 5-30 Part by weight is more preferred. When the content of the photocurable compound is excessively large, the fluidity of the pressure-sensitive adhesive before curing is increased, which may cause a decrease in handling properties and contamination.
光硬化性粘着剤は、粘着剤組成物中に光ラジカル発生剤を含有することが好ましい。光ラジカル発生剤としては、１個または複数のラジカル発生点を分子中に有する化合物が用いられ、例えば、ヒドロキシケトン類、ベンジルジメチルケタール類、アミノケトン類、アシルフォスフィンオキサイド系、ベンゾフェノン系、トリクロロメチル基含有トリアジン誘導体等が挙げられる。光ラジカル発生剤は、単独で使用してもよく、また２種以上を混合して使用してもよい。また、単官能型光ラジカル発生剤と多官能型光ラジカル発生剤とを適宜併用してもよい。光ラジカル発生剤の含有量は、粘着剤組成物の全固形分１００重量部に対して、０．０１〜１０重量部が好ましく、０．０５〜８重量部がより好ましい。 The photocurable pressure-sensitive adhesive preferably contains a photoradical generator in the pressure-sensitive adhesive composition. As the photoradical generator, compounds having one or more radical generating points in the molecule are used. For example, hydroxyketones, benzyldimethylketals, aminoketones, acylphosphine oxides, benzophenones, trichloromethyl And group-containing triazine derivatives. The photoradical generator may be used alone or in combination of two or more. A monofunctional photoradical generator and a polyfunctional photoradical generator may be used in combination as appropriate. The content of the photo radical generator is preferably 0.01 to 10 parts by weight and more preferably 0.05 to 8 parts by weight with respect to 100 parts by weight of the total solid content of the pressure-sensitive adhesive composition.
［粘着剤層の形成］
粘着剤層の形成方法としては、各種方法が用いられる。具体的には、例えば、ロールコート、キスロールコート、グラビアコート、リバースコート、ロールブラッシュ、スプレーコート、ディップロールコート、バーコート、ナイフコート、エアーナイフコート、カーテンコート、リップコート、ダイコーター等による押出しコート法等の方法が挙げられる。これらの中でも、ダイコーターを使用することが好ましく、特にファウンテンダイ、スロットダイを用いるダイコーターを使用することがより好ましい。
[Formation of adhesive layer]
Various methods are used as a method of forming the pressure-sensitive adhesive layer. Specifically, for example, by roll coat, kiss roll coat, gravure coat, reverse coat, roll brush, spray coat, dip roll coat, bar coat, knife coat, air knife coat, curtain coat, lip coat, die coater, etc. Examples thereof include an extrusion coating method. Among these, it is preferable to use a die coater, and it is particularly preferable to use a die coater using a fountain die or a slot die.
塗布後の粘着剤を乾燥させる方法としては、目的に応じて、適宜、適切な方法が採用され得る。加熱乾燥温度は、好ましくは４０℃〜２００℃であり、さらに好ましくは、５０℃〜１８０℃であり、特に好ましくは７０℃〜１７０℃である。乾燥時間は、適宜、適切な時間が採用され得る。乾燥時間は、好ましくは５秒〜２０分、さらに好ましくは５秒〜１５分、特に好ましくは１０秒〜１０分である。 As a method for drying the pressure-sensitive adhesive after application, an appropriate method can be appropriately employed depending on the purpose. The heat drying temperature is preferably 40 ° C to 200 ° C, more preferably 50 ° C to 180 ° C, and particularly preferably 70 ° C to 170 ° C. As the drying time, an appropriate time can be adopted as appropriate. The drying time is preferably 5 seconds to 20 minutes, more preferably 5 seconds to 15 minutes, and particularly preferably 10 seconds to 10 minutes.
［粘着剤層の物性］
粘着剤層は、２５℃における貯蔵弾性率Ｇ’２５℃が、１．０×１０４Ｐａ〜１．０×１０７Ｐａであることが好ましく、３．０×１０４Ｐａ〜７．０×１０６Ｐａであることがより好ましく、５．０×１０４Ｐａ〜５．０×１０６Ｐａであることがさらに好ましい。２５℃（常温）における貯蔵弾性率が過度に小さいと、粘着剤層をカットする際や、貼り合せの際の加圧によって、端面から粘着剤がはみ出して、汚染等の不具合を招く場合がある。一方、２５℃における貯蔵弾性率が過度に大きいと、カット時またはカット後に、粘着剤の端面（カット面）において、割れや欠けが発生し易くなる傾向がある。
[Physical properties of adhesive layer]
The pressure-sensitive adhesive layer preferably has a storage elastic modulus G ′ at 25 ° C. of 25 ° C. of 1.0 × 10 4 Pa to 1.0 × 10 7 Pa, and 3.0 × 10 4 Pa to 7.0 ×. 10 6 Pa is more preferable, and 5.0 × 10 4 Pa to 5.0 × 10 6 Pa is even more preferable. If the storage elastic modulus at 25 ° C. (room temperature) is excessively small, the pressure-sensitive adhesive may protrude from the end surface due to pressure applied when the pressure-sensitive adhesive layer is cut or bonded, leading to problems such as contamination. . On the other hand, if the storage elastic modulus at 25 ° C. is excessively large, cracks and chips tend to occur on the end face (cut face) of the pressure-sensitive adhesive during or after cutting.
粘着剤層は、８０℃における貯蔵弾性率Ｇ’８０℃が、１．０×１０２Ｐａ〜１．０×１０５Ｐａであることが好ましい。粘着剤層のＧ’８０℃は、５．０×１０４Ｐａ以下がより好ましく、３．０×１０４Ｐａ以下がさらに好ましく、１．０×１０４Ｐａ以下が特に好ましい。Ｇ’ ８０℃を前記範囲とすることで、加熱環境における粘着剤層の流動性が適宜の範囲となる。そのため、被着体（例えば、図１の前面透明板７０）が、印刷部７０ａ等の段差や隆起等を有している場合でも、粘着剤層の形状が段差形状に追従し、気泡の混入が抑制される。また、常温で貼り合わせが行われる場合でも、粘着剤層のＧ’８０℃が１．０×１０５Ｐａ以下であれば、貼り合わせ後の加熱によって、貼り合わせ時に混入した段差付近の気泡を効果的に除去できる。
The pressure-sensitive adhesive layer preferably has a storage elastic modulus G ′ at 80 ° C. of 80 ° C. of 1.0 × 10 2 Pa to 1.0 × 10 5 Pa. G ′ 80 ° C. of the pressure-sensitive adhesive layer is more preferably 5.0 × 10 4 Pa or less, further preferably 3.0 × 10 4 Pa or less, and particularly preferably 1.0 × 10 4 Pa or less. By making G '80 degreeC into the said range, the fluidity | liquidity of the adhesive layer in a heating environment becomes an appropriate range. Therefore, even when the adherend (for example, the front
粘着剤層の貯蔵弾性率は、ベースポリマーの構造や分子量、添加剤の種類や含有量等を調整することにより、上記範囲に調整し得る。特に、本発明では、所定の軟化点を有する水素添加型テルペンフェノール樹脂からなる粘着付与剤が用いられることで、粘着剤層の弾性率に上記の温度依存性を付与できる。すなわち、２５℃（常温）では、粘着付与剤の軟化点以下であるために、粘着剤層の弾性率が高く、加熱時には粘着付与剤が軟化するために、高温での弾性率が小さくなる。 The storage elastic modulus of the pressure-sensitive adhesive layer can be adjusted to the above range by adjusting the structure and molecular weight of the base polymer, the type and content of the additive, and the like. In particular, in the present invention, by using a tackifier made of a hydrogenated terpene phenol resin having a predetermined softening point, the above temperature dependency can be imparted to the elastic modulus of the pressure-sensitive adhesive layer. That is, at 25 ° C. (normal temperature), the elastic modulus of the pressure-sensitive adhesive layer is high because it is below the softening point of the tackifier, and the elastic modulus at high temperature decreases because the tackifier softens during heating.
また、本発明では、粘着剤層がタッチパネルや前面透明板等の被着体と貼り合わせられる際の８０℃貯蔵弾性率が、画像表示装置形成後の最終製品における粘着剤層の８０℃貯蔵弾性率よりも小さいことが好ましい。例えば、光硬化性あるいは熱硬化性の粘着剤を用いる場合、硬化前に貼り合わせを行えば、粘着剤層は適度の接着性および流動性を有する。一方、貼り合せ時やオートクレーブ等で加熱処理を行った後に、活性光線照射や加熱により粘着剤の硬化を行うことで、粘着剤層の貯蔵弾性率を大きくして、粘着剤層の剥がれ等の不具合を抑制できる。 In the present invention, the 80 ° C. storage elastic modulus when the adhesive layer is bonded to an adherend such as a touch panel or a front transparent plate is 80 ° C. storage elasticity of the adhesive layer in the final product after the image display device is formed. It is preferable to be smaller than the rate. For example, when using a photo-curing or thermosetting pressure-sensitive adhesive, the pressure-sensitive adhesive layer has appropriate adhesiveness and fluidity if bonded together before curing. On the other hand, after performing heat treatment at the time of pasting or autoclave, etc., by curing the pressure sensitive adhesive by irradiation with actinic light or heating, the storage elastic modulus of the pressure sensitive adhesive layer is increased, and the pressure sensitive adhesive layer is peeled off, etc. Defects can be suppressed.
特に、貼り合せ時の接着性および流動性と、画像表示装置形成後における接着の信頼性とを両立する観点から、粘着剤層は、硬化後の８０℃における貯蔵弾性率Ｇ’８０℃が、１．０×１０３Ｐａ〜１．０×１０６Ｐａであることが好ましく、３．０×１０３Ｐａ〜７．０×１０５Ｐａであることがより好ましく、５．０×１０３Ｐａ〜５．０×１０５Ｐａであることがさらに好ましい。また、貼り合せ時の接着性および流動性と、画像表示装置形成後の接着信頼性とを両立する観点から、粘着剤層の硬化後のＧ’８０℃は、硬化前のＧ’８０℃の２倍以上が好ましく、３倍以上がより好ましく、５倍以上がさらに好ましい。 In particular, the adhesive layer has a storage elastic modulus G ′ of 80 ° C. at 80 ° C. after curing, from the viewpoint of achieving both adhesion and fluidity at the time of bonding and reliability of adhesion after formation of the image display device. it is preferably 1.0 × 10 3 Pa~1.0 × 10 6 Pa, more preferably from 3.0 × 10 3 Pa~7.0 × 10 5 Pa, 5.0 × 10 3 Pa More preferably, it is -5.0 * 10 < 5 > Pa. Further, from the viewpoint of achieving both adhesion and fluidity at the time of bonding and adhesion reliability after formation of the image display device, G ′ 80 ° C. after curing of the pressure-sensitive adhesive layer is G ′ 80 ° C. before curing. It is preferably 2 times or more, more preferably 3 times or more, and further preferably 5 times or more.
［粘着剤の用途］
前述のように、本発明の粘着剤は、画像表示パネルとタッチパネルとの間、タッチパネルと前面透明板との間、画像表示パネルと前面透明板との間の層間充填剤として好適に用いられる。粘着剤層は、実用に供するまでの間、粘着剤層の露出面を保護する目的で、必要に応じて、保護シートが剥離可能に貼着されることが好ましい。保護シートの構成材料としては、例えば、ポリエチレン、ポリプロピレン、ポリエチレンテレフタレート、ポリエステルフィルム等のプラスチックフィルム、紙、布、不織布等の多孔質材料、ネット、発泡シート、金属箔、およびこれらのラミネート体等の適宜な薄葉体等が挙げられる。表面平滑性に優れる点からプラスチックフィルムが好適に用いられる。
[Use of adhesive]
As described above, the pressure-sensitive adhesive of the present invention is suitably used as an interlayer filler between the image display panel and the touch panel, between the touch panel and the front transparent plate, and between the image display panel and the front transparent plate. For the purpose of protecting the exposed surface of the pressure-sensitive adhesive layer until the pressure-sensitive adhesive layer is put to practical use, it is preferable that the protective sheet is attached in a peelable manner as necessary. As a constituent material of the protective sheet, for example, plastic films such as polyethylene, polypropylene, polyethylene terephthalate, and polyester films, porous materials such as paper, cloth, and nonwoven fabric, nets, foam sheets, metal foils, and laminates thereof, etc. Appropriate thin leaves and the like can be mentioned. A plastic film is preferably used from the viewpoint of excellent surface smoothness.
保護シート付き粘着剤層は、必要に応じて所望サイズにカットされて実用に供される。一般には、長尺状に形成された保護シート付き粘着剤層が、画像表示装置のサイズ（画面サイズ）と合致する製品サイズにカットされる。カット方法としては、トムソン刃等を用いて打ち抜く方法や、丸刃および皿刃等のカッターや、レーザー光、水圧を利用する方法等が挙げられる。 The pressure-sensitive adhesive layer with a protective sheet is cut into a desired size as necessary and provided for practical use. In general, an adhesive layer with a protective sheet formed in a long shape is cut into a product size that matches the size (screen size) of the image display device. Examples of the cutting method include a method of punching using a Thomson blade and the like, a cutter such as a round blade and a countersink, a method of using laser light and water pressure, and the like.
画像表示装置の形成において、粘着剤層の貼り合せ手順や、貼り合わせ方法等は特に限定されない。図１に示す前面透明板７０における印刷部７０ａのような非平坦部を有する部材との貼り合わせに際しては、印刷部７０ａ等の非平坦部付近の気泡を除去するために、脱泡が行われることが好ましい。脱泡方法としては、加熱、加圧、減圧等の適宜の方法が採用され得る。例えば、減圧・加熱下で気泡の混入を抑制しながら貼り合わせが行われ、その後、ディレイバブルの抑制等を目的として、オートクレーブ処理等により、加熱と同時に加圧が行われることが好ましい。加熱により脱泡が行われる場合、加熱温度は、一般的に３０℃〜１５０℃程度、好ましくは４０°〜１３０℃、より好ましくは５０℃〜１２０℃、さらに好ましくは６０℃〜１００℃の範囲である。また、加圧が行われる場合、圧力は一般に０．０５ＭＰａ〜２ＭＰａ程度、好ましくは０．１ＭＰａ〜１．５ＭＰａ，より好ましくは０．２ＭＰａ〜１ＭＰａの範囲内である。
In the formation of the image display device, the bonding procedure of the pressure-sensitive adhesive layer, the bonding method, and the like are not particularly limited. When the front
以下に実施例および比較例を挙げてさらに説明するが、本発明は、これらの実施例に限定されるものではない。 The present invention will be further described below with reference to examples and comparative examples, but the present invention is not limited to these examples.
［合成例］
＜合成例１＞
温度計、攪拌機、還流冷却管および窒素ガス導入管を備えたセパラブルフラスコに、２−エチルヘキシルアクリレート（２ＥＨＡ）を７５重量部、Ｎ−ビニルピロリドン（ＮＶＰ）を２５重量部、重合開始剤としてアゾビスイソブチロニトリル（ＡＩＢＮ）を０．２重量部、および酢酸エチル２３３重量部を投入した後、窒素ガスを流し、攪拌しながら約１時間窒素置換を行った。その後、７０℃にフラスコを加熱し、５時間反応させて重量平均分子量（Ｍｗ）８０万のアクリル系ポリマーを得た（以下、このベースポリマーを「ポリマー１」と称する）。
[Synthesis example]
<Synthesis Example 1>
In a separable flask equipped with a thermometer, stirrer, reflux condenser and nitrogen gas inlet tube, 75 parts by weight of 2-ethylhexyl acrylate (2EHA), 25 parts by weight of N-vinylpyrrolidone (NVP), azo as a polymerization initiator After 0.2 parts by weight of bisisobutyronitrile (AIBN) and 233 parts by weight of ethyl acetate were added, nitrogen substitution was performed for about 1 hour while flowing nitrogen gas and stirring. Thereafter, the flask was heated to 70 ° C. and reacted for 5 hours to obtain an acrylic polymer having a weight average molecular weight (Mw) of 800,000 (hereinafter, this base polymer is referred to as “polymer 1”).
＜合成例２＞
温度計、攪拌機、還流冷却管および窒素ガス導入管を備えたセパラブルフラスコに、２ＥＨＡを６５重量部、メタクリル酸メチル（ＭＭＡ）を１０重量部、ＮＶＰを１５重量部、ヒドロキシエチルアクリレート（ＨＥＡ）を１０重量部、重合開始剤としてＡＩＢＮを０．２重量部、および酢酸エチル２３３重量部を投入した後、窒素ガスを流し、攪拌しながら約１時間窒素置換を行った。その後、７０℃にフラスコを加熱し、５時間反応させて重量平均分子量（Ｍｗ）８０万のアクリル系ポリマーを得た（以下、このベースポリマーを「ポリマー２」と称する）。
<Synthesis Example 2>
In a separable flask equipped with a thermometer, a stirrer, a reflux condenser, and a nitrogen gas inlet tube, 65 parts by weight of 2EHA, 10 parts by weight of methyl methacrylate (MMA), 15 parts by weight of NVP, and hydroxyethyl acrylate (HEA) 10 parts by weight, AIBN 0.2 parts by weight as a polymerization initiator, and 233 parts by weight of ethyl acetate were added, and nitrogen substitution was performed for about 1 hour while flowing nitrogen gas and stirring. Thereafter, the flask was heated to 70 ° C. and reacted for 5 hours to obtain an acrylic polymer having a weight average molecular weight (Mw) of 800,000 (hereinafter, this base polymer is referred to as “polymer 2”).
［実施例１，２、および比較例１〜５］
上記ポリマー１，２をベースポリマーとして用い、表１に示す化合物を混合溶解して、粘着剤組成物を調整した（表１中の粘着剤組成の数字は、いずれも重量部）。調整した粘着剤組成物溶液を、ＰＥＴセパレータ上に、乾燥後厚みが１００μｍとなるように塗布・乾燥して、粘着剤層を得た。
なお、表１において、粘着付与剤１（ＹＳポリスターＮＨ）は、ヤスハラケミカル製の水素添加型テルペンフェノール樹脂であり、軟化点は１３０℃、テルペン比率は０．５モルである。粘着付与剤２（ＹＳポリスターＵＨ）は、ヤスハラケミカル製の水素添加型テルペンフェノール樹脂であり、軟化点は１１５℃、テルペン比率は０．８モルである。粘着付与剤３（ＹＳレジン ＳＸ１００）は、ヤスハラケミカル製のスチレンオリゴマーであり、軟化点は１００℃である。粘着付与剤４（パインクリスタル ＫＥ−３１１）は、荒川化学工業製の水素化ロジンエステルであり、軟化点は９５℃である。光硬化性化合物（ＮＫエステル ＡＰＧ‐４００）は、新中村化学工業製のポリエチレングリコールジアクリレート（二官能アクリレート）である。重合開始剤（イルガキュア１８４）は、チバスペシャリティケミカル製のアルキルフェノン系の光重合開始剤である。
[Examples 1 and 2 and Comparative Examples 1 to 5]
Using the polymers 1 and 2 as the base polymer, the compounds shown in Table 1 were mixed and dissolved to prepare an adhesive composition (the numbers of the adhesive composition in Table 1 are all parts by weight). The prepared pressure-sensitive adhesive composition solution was applied and dried on a PET separator so that the thickness after drying was 100 μm, to obtain a pressure-sensitive adhesive layer.
In Table 1, tackifier 1 (YS Polystar NH) is a hydrogenated terpene phenol resin manufactured by Yasuhara Chemical, and has a softening point of 130 ° C. and a terpene ratio of 0.5 mol. Tackifier 2 (YS Polystar UH) is a hydrogenated terpene phenol resin manufactured by Yasuhara Chemical, having a softening point of 115 ° C. and a terpene ratio of 0.8 mol. Tackifier 3 (YS Resin SX100) is a styrene oligomer made by Yasuhara Chemical, and has a softening point of 100 ° C. Tackifier 4 (Pine Crystal KE-311) is a hydrogenated rosin ester manufactured by Arakawa Chemical Industries, and has a softening point of 95 ° C. The photocurable compound (NK ester APG-400) is polyethylene glycol diacrylate (bifunctional acrylate) manufactured by Shin-Nakamura Chemical Co., Ltd. The polymerization initiator (Irgacure 184) is an alkylphenone photopolymerization initiator manufactured by Ciba Specialty Chemicals.
［評価］
＜評価用疑似画像表示装置の作製＞
平坦なガラス板（０．７ｍｍ×５０ｍｍ×１００ｍｍ）に、各実施例および比較例で得られた粘着剤層を貼り合わせた後、ＰＥＴセパレータを剥離した。セパレータ剥離後の粘着剤の露出面上に、黒色インク（厚み２０μｍ）が周縁部に枠状に印刷されたガラス板（０．７ｍｍ×５０ｍｍ×１００ｍｍ、インク印刷幅：端部から１０ｍｍ）を、印刷面と粘着剤層が接するよう載置した後、真空熱圧着装置で熱圧着して貼り合せを行った（温度８０℃、圧力０．３ＭＰａ、圧力保持時間５秒）。その後、オートクレーブ処理を行った（５０℃、０．５ＭＰａ、３０分）。実施例２のみ、オートクレーブ処理後に、ガラス板側からメタルハライドランプ（３００ｍＷ／ｃｍ２）で紫外線を照射し、光硬化性粘着剤の硬化を行った（積算光量：３０００ｍＪ／ｃｍ２）。このようにして、評価用疑似画像表示装置が得られた。
[Evaluation]
<Production of pseudo image display device for evaluation>
After sticking the adhesive layer obtained by each Example and the comparative example to the flat glass plate (0.7 mm x 50 mm x 100 mm), the PET separator was peeled. A glass plate (0.7 mm × 50 mm × 100 mm, ink printing width: 10 mm from the end) on which the black ink (thickness 20 μm) is printed in a frame shape on the periphery on the exposed surface of the adhesive after peeling the separator, After placing the printed surface and the pressure-sensitive adhesive layer in contact, bonding was performed by thermocompression bonding with a vacuum thermocompression bonding apparatus (temperature 80 ° C., pressure 0.3 MPa, pressure holding time 5 seconds). Then, the autoclave process was performed (50 degreeC, 0.5 MPa, 30 minutes). Only in Example 2, after the autoclave treatment, ultraviolet rays were irradiated from the glass plate side with a metal halide lamp (300 mW / cm 2 ) to cure the photocurable adhesive (integrated light amount: 3000 mJ / cm 2 ). In this way, a pseudo image display device for evaluation was obtained.
＜気泡の評価＞
評価用疑似画像表示装置の黒色インク印刷部の内側近傍を、倍率２０倍のデジタルマイクロスコープで観察し、粘着剤層中の気泡の有無を確認した（初期評価）。また、８５℃のオーブンに４８時間投入後、同様の方法で気泡の有無を確認した。
<Evaluation of bubbles>
The vicinity of the inner side of the black ink printing portion of the evaluation pseudo image display device was observed with a digital microscope with a magnification of 20 times to confirm the presence or absence of bubbles in the adhesive layer (initial evaluation). Further, after being put into an 85 ° C. oven for 48 hours, the presence or absence of bubbles was confirmed by the same method.
＜白濁＞
上記の試料（評価用疑似画像表示装置）における、粘着剤層の白濁の有無を目視で確認した(初期評価)。６０℃９５％ＲＨの恒温恒湿槽内に、試料を２４０時間投入した。その後、試料後取り出し、２５℃５０％の環境下で２４時間保管後に、粘着剤層の白濁の有無を目視で確認した。
<White turbidity>
In the above sample (pseudo image display device for evaluation), the presence or absence of cloudiness of the pressure-sensitive adhesive layer was visually confirmed (initial evaluation). The sample was put in a constant temperature and humidity chamber at 60 ° C. and 95% RH for 240 hours. Thereafter, the sample was taken out and stored for 24 hours in an environment of 25 ° C. and 50%, and the presence or absence of white turbidity of the pressure-sensitive adhesive layer was visually confirmed.
上記各実施例および比較例の粘着剤層の組成、および各評価結果の一覧を表１に示す。 Table 1 shows the composition of the pressure-sensitive adhesive layers of the above Examples and Comparative Examples, and a list of evaluation results.
粘着付与剤１を含有する粘着剤が用いられた実施例１，２は、いずれも気泡がなく、かつ高温高湿環境に暴露後も白濁が生じていなかった。粘着付与剤を含有しない粘着剤が用いられた比較例１，２では、粘着剤の白濁は生じなかったが、印刷部（段差）付近で気泡が発生していた。 In Examples 1 and 2 in which the pressure-sensitive adhesive containing the tackifier 1 was used, neither air bubbles nor white turbidity was generated after exposure to a high temperature and high humidity environment. In Comparative Examples 1 and 2 in which a pressure-sensitive adhesive containing no tackifier was used, white turbidity of the pressure-sensitive adhesive did not occur, but bubbles were generated in the vicinity of the printing portion (step).
一方、比較例３〜５では、軟化点が所定範囲内の粘着付与剤を含有する粘着剤が用いられたため、気泡は発生していなかった。しかしながら、テルペンのモル比率が０．８である粘着付与剤２が用いられた比較例３では、高温高湿環境に暴露する前から粘着剤の白濁が生じていた。これは、粘着剤を構成するアクリル系ベースポリマーと、テルペン比率の高い水素添加型テルペンフェノールとの相溶性が低いことに起因すると推定される。また、比較例４，５では、初期では白濁が生じていなかったものの、高温高湿環境に暴露後の粘着剤層に白濁が見られた。 On the other hand, in Comparative Examples 3 to 5, since an adhesive containing a tackifier having a softening point within a predetermined range was used, no bubbles were generated. However, in Comparative Example 3 in which the tackifier 2 having a terpene molar ratio of 0.8 was used, the adhesive had become cloudy before being exposed to a high temperature and high humidity environment. This is presumably due to the low compatibility between the acrylic base polymer constituting the pressure-sensitive adhesive and the hydrogenated terpene phenol having a high terpene ratio. In Comparative Examples 4 and 5, although no white turbidity occurred at the initial stage, white turbidity was observed in the pressure-sensitive adhesive layer after exposure to a high temperature and high humidity environment.
以上の結果から、所定の粘着性付与剤を含有する粘着剤のみが、層間充填剤として用いた場合における、段差追従性と、高温高湿環境暴露時の白濁抑止の両方を満足し得ることが分かる。 From the above results, it is possible that only the pressure-sensitive adhesive containing the predetermined tackifier can satisfy both the step following ability and the white turbidity suppression when exposed to a high temperature and high humidity environment when used as an interlayer filler. I understand.
１０ ：画像表示パネル
２１，２２：粘着剤層（層間充填剤）
３０ ：タッチパネル
７０ ：前面透明板
１００ ：画像表示装置
10:
30: Touch panel 70: Front transparent plate 100: Image display device
Claims (3)
アクリル系ベースポリマーと、軟化点が７０℃〜１５０℃の水素添加型テルペンフェノール樹脂とを含有し、
前記水素添加型テルペンフェノール樹脂は、テルペンのモル比率が０．１〜０．７であり、
粘着剤組成物の全量１００重量部に対する、前記アクリル系ベースポリマーの含有量が４５〜９５重量部であり、かつ、前記アクリル系ベースポリマーと前記水素添加型テルペンフェノール樹脂の含有量の合計が、７０重量部以上である、粘着剤。 An adhesive used between the front transparent plate and the touch panel, between the front transparent plate and the image display panel, or between the touch panel and the image display panel,
Containing an acrylic base polymer and a hydrogenated terpene phenol resin having a softening point of 70 ° C to 150 ° C,
The hydrogenated terpene phenol resin has a terpene molar ratio of 0.1 to 0.7,
The content of the acrylic base polymer is 45 to 95 parts by weight relative to 100 parts by weight of the total amount of the pressure-sensitive adhesive composition, and the total content of the acrylic base polymer and the hydrogenated terpene phenol resin is The adhesive which is 70 weight part or more.
前記前面透明板と前記タッチパネルとの間、前記前面透明板と前記画像表示パネルとの間、および前記タッチパネルと前記画像表示パネルとの間のいずれかに、請求項１または２に記載の粘着剤からなる粘着剤層を備える、画像表示装置。 At least one of a touch panel and a front transparent plate is provided on the surface of the image display panel,
The pressure-sensitive adhesive according to claim 1 or 2, between the front transparent plate and the touch panel, between the front transparent plate and the image display panel, and between the touch panel and the image display panel. An image display device comprising an adhesive layer comprising:
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013075184A JP6073173B2 (en) | 2013-03-29 | 2013-03-29 | Adhesive and image display device using the same |
| US14/771,524 US20160002505A1 (en) | 2013-03-29 | 2014-03-12 | Pressure sensitive adhesive and image display device using the same |
| KR1020157024006A KR102248655B1 (en) | 2013-03-29 | 2014-03-12 | Tackifying agent and image display device using this adhesive |
| PCT/JP2014/056462 WO2014156641A1 (en) | 2013-03-29 | 2014-03-12 | Tackifying agent and image display device using this adhesive |
| CN201480018762.2A CN105073935B (en) | 2013-03-29 | 2014-03-12 | Adhesive and the image display device using the adhesive |
| TW103111307A TWI588227B (en) | 2013-03-29 | 2014-03-26 | Adhesive and image display device using the same |
| TW106116025A TW201726872A (en) | 2013-03-29 | 2014-03-26 | Pressure sensitive adhesive and image display device using the same |
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| JP2017000069A Division JP2017101246A (en) | 2017-01-04 | 2017-01-04 | Pressure sensitive adhesive and image display device using the same |
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| JP6073173B2 JP6073173B2 (en) | 2017-02-01 |
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| US (1) | US20160002505A1 (en) |
| JP (1) | JP6073173B2 (en) |
| KR (1) | KR102248655B1 (en) |
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| JP2017002119A (en) * | 2015-06-04 | 2017-01-05 | 日東電工株式会社 | Adhesive sheet, optical film with adhesive agent and manufacturing method of image display unit |
| CN106867418A (en) * | 2015-10-13 | 2017-06-20 | 日东电工株式会社 | Bonding sheet, the polarization plates with adhesive phase and image display device |
| WO2017110839A1 (en) * | 2015-12-21 | 2017-06-29 | 積水化学工業株式会社 | Adhesive composition and adhesive tape |
| WO2019004160A1 (en) * | 2017-06-26 | 2019-01-03 | 大日本印刷株式会社 | Light modulating member, sun visor, and movable body |
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| JP6526951B2 (en) * | 2014-08-29 | 2019-06-05 | スリーエム イノベイティブ プロパティズ カンパニー | Optically transparent adhesive and optical laminate |
| JP6538332B2 (en) * | 2014-11-17 | 2019-07-03 | 日東電工株式会社 | Optical double-sided adhesive sheet |
| KR20180068947A (en) * | 2015-10-07 | 2018-06-22 | 세키스이가가쿠 고교가부시키가이샤 | Interlayer filler material for touch panels, and touch panel laminate |
| KR20220078379A (en) * | 2020-12-03 | 2022-06-10 | 엘지디스플레이 주식회사 | Display device |
| WO2024134438A1 (en) * | 2022-12-22 | 2024-06-27 | 3M Innovative Properties Company | Adhesive film with clean removal after aging |
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Also Published As
| Publication number | Publication date |
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| US20160002505A1 (en) | 2016-01-07 |
| KR20150138183A (en) | 2015-12-09 |
| KR102248655B1 (en) | 2021-05-04 |
| TW201446910A (en) | 2014-12-16 |
| CN105073935A (en) | 2015-11-18 |
| JP6073173B2 (en) | 2017-02-01 |
| WO2014156641A1 (en) | 2014-10-02 |
| TW201726872A (en) | 2017-08-01 |
| CN105073935B (en) | 2017-09-26 |
| TWI588227B (en) | 2017-06-21 |
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